The C type natriuretic peptide receptor tethers AHNAK1 at the plasma membrane to potentiate arachidonic acid-induced calcium mobilization

被引:24
作者
Alli, Abdel A. [1 ,2 ,3 ]
Gower, William R., Jr. [1 ,2 ,3 ]
机构
[1] James A Haley Vet Hosp, Res Serv, Tampa, FL 33612 USA
[2] Univ S Florida, Coll Med, Dept Mol Med, Tampa, FL USA
[3] Univ S Florida, Cardiac Hormone Ctr, Tampa, FL USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2009年 / 297卷 / 05期
关键词
3T3-L1; smooth muscle cells; rat gastric muscosa cell 1; phospholipase C; CYTOSOLIC PHOSPHOLIPASE A(2); ACTIVATED PROTEIN-KINASE; CLEARANCE FUNCTION; DNA-SYNTHESIS; CELL-LINE; EXPRESSION; DECREASE; MUSCLE; DOMAIN; HEART;
D O I
10.1152/ajpcell.00219.2009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alli AA, Gower WR, Jr. The C type natriuretic peptide receptor tethers AHNAK1 at the plasma membrane to potentiate arachidonic acid-induced calcium mobilization. Am J Physiol Cell Physiol 297: C1157-C1167, 2009. First published August 26, 2009; doi:10.1152/ajpcell.00219.2009.-Arachidonic acid (AA) liberated from membrane phospholipids is known to activate phospholipase C gamma 1 (PLC gamma 1) concurrently with AHNAK in nonneuronal cells. The recruitment of AHNAK from the nucleus is required for it to activate PLC gamma 1 at the plasma membrane. Here, we identify the C-type natriuretic peptide receptor (NPR-C), an atypical G protein-coupled receptor, as a protein binding partner for AHNAK1 in various cell types. Mass spectrometry and MASCOT analysis of excised bands from NPR-C immunoprecipitation studies revealed multiple signature peptides corresponding to AHNAK1. Glutathione S-transferase (GST) pulldown assays using GST-AHNAK1 fusion proteins corresponding to each of the distinct domains of AHNAK1 showed the C1 domain of AHNAK1 associates with NPR-C. The role of NPR-C in mediating AA-dependent AHNAK1 calcium signaling was explored in various cell types, including 3T3-L1 preadipocytes during the early stages of differentiation. Sucrose density gradient centrifugation studies showed AHNAK1 resides in the nucleus, cytoplasm, and at the plasma membrane, but small interfering RNA (siRNA)-mediated knockdown of NPR-C resulted in AHNAK1 accumulation in the nucleus. Overexpression of a portion of AHNAK1 resulted in augmentation of intracellular calcium mobilization, whereas siRNA-mediated knockdown of NPR-C or AHNAK1 protein resulted in attenuation of intracellular calcium mobilization in response to phorbol 12-myristate 13-acetate. We characterize the novel association between AHNAK1 and NPR-C and provide evidence that this association potentiates the AA-induced mobilization of intracellular calcium. We address the role of intracellular calcium in the various cell types that AHNAK1 and NPR-C were found to associate.
引用
收藏
页码:C1157 / C1167
页数:11
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